Au-catalyzed skeletal rearrangement of O-propargylic oximes via N–O bond cleavage with the aid of a Brønsted base cocatalyst
Author:
Affiliation:
1. Department of Chemistry
2. Graduate School of Science
3. Tohoku University
4. Sendai
5. Japan
6. Research and Analytical Center for Giant Molecules
Abstract
Au-catalyzed skeletal rearrangement reaction of O-propargylic oxime proceeded via N–O bond cleavage with the aid of a Brønsted base cocatalyst.
Funder
Japan Society for the Promotion of Science
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2019/SC/C9SC00501C
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5. Cycloisomerization of 1,n-Enynes: Challenging Metal-Catalyzed Rearrangements and Mechanistic Insights
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